
Pro Med Mfg., Inc.
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FT MODEL TABLE W/ELECTRIC HI LO OPTION E is an FDA 510(k)-cleared medical device (K925563) manufactured by Pro Med Mfg., Inc.. This device is classified under the Physical Medicine specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on May 25, 1993. Regulation: 8.

Synthes (Usa)
SKU K100676
BackorderedMedline
SKU VM-1270020

Cardinal Health
SKU VM-1270026
BackorderedMoog
SKU VM-1270057